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8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies

The dihydroneopterin aldolase (DHNA, EC 4.1.2.25) activity of FolB protein is required for the conversion of 7,8-dihydroneopterin (DHNP) to 6-hydroxymethyl-7,8-dihydropterin (HP) and glycolaldehyde (GA) in the folate pathway. FolB protein from Mycobacterium tuberculosis (MtFolB) is essential for bac...

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Autores principales: Czeczot, Alexia de Matos, Roth, Candida Deves, Ducati, Rodrigo Gay, Pissinate, Kenia, Rambo, Raoní Scheibler, Timmers, Luís Fernando Saraiva Macedo, Abbadi, Bruno Lopes, Macchi, Fernanda Souza, Pestana, Víctor Zajaczkowski, Basso, Luiz Augusto, Machado, Pablo, Bizarro, Cristiano Valim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993393/
https://www.ncbi.nlm.nih.gov/pubmed/33752554
http://dx.doi.org/10.1080/14756366.2021.1900157
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author Czeczot, Alexia de Matos
Roth, Candida Deves
Ducati, Rodrigo Gay
Pissinate, Kenia
Rambo, Raoní Scheibler
Timmers, Luís Fernando Saraiva Macedo
Abbadi, Bruno Lopes
Macchi, Fernanda Souza
Pestana, Víctor Zajaczkowski
Basso, Luiz Augusto
Machado, Pablo
Bizarro, Cristiano Valim
author_facet Czeczot, Alexia de Matos
Roth, Candida Deves
Ducati, Rodrigo Gay
Pissinate, Kenia
Rambo, Raoní Scheibler
Timmers, Luís Fernando Saraiva Macedo
Abbadi, Bruno Lopes
Macchi, Fernanda Souza
Pestana, Víctor Zajaczkowski
Basso, Luiz Augusto
Machado, Pablo
Bizarro, Cristiano Valim
author_sort Czeczot, Alexia de Matos
collection PubMed
description The dihydroneopterin aldolase (DHNA, EC 4.1.2.25) activity of FolB protein is required for the conversion of 7,8-dihydroneopterin (DHNP) to 6-hydroxymethyl-7,8-dihydropterin (HP) and glycolaldehyde (GA) in the folate pathway. FolB protein from Mycobacterium tuberculosis (MtFolB) is essential for bacilli survival and represents an important molecular target for drug development. S8-functionalized 8-mercaptoguanine derivatives were synthesised and evaluated for inhibitory activity against MtFolB. The compounds showed IC(50) values in the submicromolar range. The inhibition mode and inhibition constants were determined for compounds that exhibited the strongest inhibition. Additionally, molecular docking analyses were performed to suggest enzyme-inhibitor interactions and ligand conformations. To the best of our knowledge, this study describes the first class of MtFolB inhibitors.
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spelling pubmed-79933932021-03-31 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies Czeczot, Alexia de Matos Roth, Candida Deves Ducati, Rodrigo Gay Pissinate, Kenia Rambo, Raoní Scheibler Timmers, Luís Fernando Saraiva Macedo Abbadi, Bruno Lopes Macchi, Fernanda Souza Pestana, Víctor Zajaczkowski Basso, Luiz Augusto Machado, Pablo Bizarro, Cristiano Valim J Enzyme Inhib Med Chem Research Paper The dihydroneopterin aldolase (DHNA, EC 4.1.2.25) activity of FolB protein is required for the conversion of 7,8-dihydroneopterin (DHNP) to 6-hydroxymethyl-7,8-dihydropterin (HP) and glycolaldehyde (GA) in the folate pathway. FolB protein from Mycobacterium tuberculosis (MtFolB) is essential for bacilli survival and represents an important molecular target for drug development. S8-functionalized 8-mercaptoguanine derivatives were synthesised and evaluated for inhibitory activity against MtFolB. The compounds showed IC(50) values in the submicromolar range. The inhibition mode and inhibition constants were determined for compounds that exhibited the strongest inhibition. Additionally, molecular docking analyses were performed to suggest enzyme-inhibitor interactions and ligand conformations. To the best of our knowledge, this study describes the first class of MtFolB inhibitors. Taylor & Francis 2021-03-23 /pmc/articles/PMC7993393/ /pubmed/33752554 http://dx.doi.org/10.1080/14756366.2021.1900157 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Czeczot, Alexia de Matos
Roth, Candida Deves
Ducati, Rodrigo Gay
Pissinate, Kenia
Rambo, Raoní Scheibler
Timmers, Luís Fernando Saraiva Macedo
Abbadi, Bruno Lopes
Macchi, Fernanda Souza
Pestana, Víctor Zajaczkowski
Basso, Luiz Augusto
Machado, Pablo
Bizarro, Cristiano Valim
8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
title 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
title_full 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
title_fullStr 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
title_full_unstemmed 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
title_short 8-Mercaptoguanine-based inhibitors of Mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
title_sort 8-mercaptoguanine-based inhibitors of mycobacterium tuberculosis dihydroneopterin aldolase: synthesis, in vitro inhibition and docking studies
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993393/
https://www.ncbi.nlm.nih.gov/pubmed/33752554
http://dx.doi.org/10.1080/14756366.2021.1900157
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